Clinical Research Coordinator RN

Benefits

Qualifications

• •Ability to perform clinical tasks including assisting physician, ARNP and CRN with minor procedures and other study requirements within scope of practice
• •Ability to work independently in a fast-paced clinical or research environment, handling multiple tasks simultaneously, effectively, and in an organized and timely manner [Required]
• •Ability to acclimate and integrate into various clinical settings as needed per protocol [Required]
• •Demonstrated skills in clinical competencies including physical assessment, phlebotomy, IV insertion and administration of investigational drugs in accordance with AdventHealth Policies and Procedures
• •Knowledge of HIPAA data protection and patient advocacy or similar awareness of ethical treatment of participants in research [Required]
• •Ability to communicate effectively with research participants, investigators, research staff and external partners
• •Ability to apply analytical approach to problem solving, obtain and analyze facts, and apply sound judgement
• •Ability to accept direction and respond to the changing needs of clinical research units [Required]
• •Working knowledge of Microsoft Office applications, such as Word, Excel, Access, Outlook, and Internet knowledge and skill [Required]
• •Specialized knowledge of assigned therapeutic areas as it relates to research and clinical trials
• •Associate's of Nursing [Required]
• •Nursing
• •Registered Nurse (RN) [Required]
• •Basic Life Support - CPR Cert (BLS) [Required]
• •11 more items(s)

Responsibilities

• •Executes and coordinates the informed consent process for participants in clinical trials and research studies
• •Screens potential research participants to determine eligibility for clinical trials and studies
• •Provides detailed information about the study, including its purpose, procedures, risks, and benefits, to potential participants
• •Ensures that participants fully understand the informed consent document before they sign it, and clarifies any questions or concerns
• •Maintains accurate and complete records of the informed consent process, including signed consent forms and documentation of discussions
• •Coordinates or performs biospecimen collection and maintains HIPAA protected database connecting patient information to biospecimens used in research
• •Serves as the study-specific clinical point of contact for participants, investigators, research staff, hospital departments and external research partners
• •Maintains sensitivity to cost containment measures by conserving hospital supplies and human resources while overseeing proposed project budgets
• •Conducts research regarding patient screening and clinical eligibility assessments
• •Coordinates the care and follow-up of volunteers placed on research studies, trials, and programs
• •Provides ongoing support and information to participants throughout the duration of studies
• •Ability to perform clinical tasks including assisting physician, ARNP and CRN with minor procedures and other study requirements within scope of practice
• •Ability to work independently in a fast-paced clinical or research environment, handling multiple tasks simultaneously, effectively, and in an organized and timely manner
• •Demonstrated skills in clinical competencies including physical assessment, phlebotomy, IV insertion and administration of investigational drugs in accordance with AdventHealth Policies and Procedures
• •Other duties as assigned
• •12 more items(s)